US3929847A - Ether diester derivatives of p-dioxanone - Google Patents

Ether diester derivatives of p-dioxanone Download PDF

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US3929847A
US3929847A US508314A US50831474A US3929847A US 3929847 A US3929847 A US 3929847A US 508314 A US508314 A US 508314A US 50831474 A US50831474 A US 50831474A US 3929847 A US3929847 A US 3929847A
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Jr Thomas C Snapp
Alden E Blood
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Eastman Kodak Co
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C08K5/10—Esters; Ether-esters
    • C08K5/101—Esters; Ether-esters of monocarboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C08K5/10—Esters; Ether-esters
    • C08K5/11—Esters; Ether-esters of acyclic polycarboxylic acids

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  • This invention relates to a new series of ether-diester derivatives of p-dioxanone having the formula wherein R is alkyl of from 1 to 7 carbon atoms or the phenyl moiety and R is alkyl of from 1 to 8 carbon atoms.
  • R is alkyl of from 1 to 7 carbon atoms or the phenyl moiety and R is alkyl of from 1 to 8 carbon atoms.
  • These novel compounds are produced by reacting p-dioxanone with an aliphatic alcohol having from 1 to 8 carbon atoms and esterifying the reaction product with an aliphatic carboxylic acid having from 2 to 8 carbon atoms or a corresponding acid anhydride. Benzoic acid or its anhydride yields the phenyl moiety in the ether-diester derivatives.
  • the etherdiesters are particularly useful as plasticizers for polyvinyl chloride.
  • R is alkyl of from 1 to 8 carbon atoms and R is alkyl of from 1 to 7 carbon atoms or the phenyl moiety.
  • novel ether-diesters described herein result from the selective reaction of p-dioxan-2-one (p-dioxanone) with various aliphatic alcohols to yield an intermediate hydroxy ether-ester which can then be esterified.
  • p-dioxanone p-dioxanone
  • the highly selective reaction of p-dioxan-2-one with an alcohol is unexpected, since transesterification of the hydroxyetherester product with p-dioxanone could readily occur and p-dioxanone self-condensation would be a predicted side reaction. Neither the transesterification nor the self-condensation reaction is encountered in the synthesis of the ether-diesters.
  • novel ether-diesters of this invention exhibit good utility in a broad range of applications. They have been found to be particularly effective plasticizers for polyvinyl chloride resin.
  • the plasticizer properties of these compounds are characterized by good volatility and low temperature flexibility.
  • Other application areas in which these compounds are useful include viscosity improvers for motor oil and brake fluid; and solvents in waxes, polishes and lubricants.
  • an aliphatic alcohol is reacted with the p-dioxanone to afford nearly quantitative yields of alkyl beta-hydroxyethoxyacetate.
  • This reaction is accomplished with an acid or basic catalyst to accelerate the reaction rate.
  • Suitable catalysts for this reaction in clude sulfuric acid, organotin compounds (dibutyltin oxide, dibutyltin dilaurate, etc.), hydrochloric acid, zinc chloride, p-toluenesulfonic acid, pyridine, aliphatic tertiary amines, alkali metal hydroxides and N,N-dimethylaniline.
  • the desired product can be produced in a noncatalyzed reaction between the two reactants.
  • the catalyst concentration of from about 0.01 to about 2.0 weight percent, based on the total reactant weight, should be employed.
  • a preferred catalyst concentration for this reaction is 0.1-1.0 weight percent of the total reactant weight.
  • the reaction temperature at this stage should be from about 50C. to about 150C.
  • the reaction can be conducted at a greater than atmospheric pressure without detrimental effects to the product.
  • a mole ratio of alcohol to lactone can be from about 1:1 to about 15:1, respectively.
  • a preferred ratio of reactants is from about 2:1 to about 7:1, respectively.
  • the alcohol must be aliphatic and have a carbon skeleton of from 1 to 8 carbon atoms.
  • Alcohols of particular importance are methanol, ethanol, propanol, n-butanol, isobutanol, 2-methylpentanol-l, 2-hexanol, 2-ethylhexanol-l, n-octanol, allyl alcohol and crotonyl alcohol.
  • the second step of the reaction sequence is the esterification of the intermediate alkyl beta-hydroxyethoxyacetate.
  • Esteriflcation of the hydroxylated ether-ester can be accomplished by reaction with either a carboxylic acid or an acid anhydride.
  • the carboxylic acid or anhydride is aliphatic in nature with a carbon chain of from 2 to 8 carbon atoms or aromatic with the phenyl moiety.
  • the mole ratio of hydroxylated ester to acid moiety should be from about 10:10 to about 1.0230, respectively, to insure complete esterification of the p-dioxanone diester derivative.
  • Esteriflcation with an anhydride is achieved with or without catalysis at temperatures of from about 50C. to about 150C.
  • esterification with the carboxylic acid requires a low concentration (from about 0.01 to about 1.0 weight percent based on total weight of the reactant) of acid catalyst to produce the desired diester product.
  • Suitable acid catalysts are methanesulfonic acid, p-toluenesulfonic, phosphoric acid, sulfuric acid, hydrochloric acid, and zinc chloride.
  • An azeotropic agent such as benzene, toluene, or hexane is useful to aid water removal during the reaction. Esterification temperatures with the acid should be from about 50C. to about 200C.
  • novel ether-diesters are viscous, colorless liquids or low melting solids which can be distilled at reduced pressure without decomposition. Variation in physical properties (water and organic solubilities) can be readily obtained by modification of the carbon skeleton of the alcohol or acid utilized. This available range of properties renders these products particularly useful as coalescing agents and plasticizers in coating and resin applications.
  • EXAMPLE 1 This example demonstrates the synthesis of an etherdiester of p-dioxan-Z-one by the noncatalyzed reactions of an aliphatic alcohol, p-dioxan-2-one, and an acid anhydride.
  • a one-liter, four-neck flask is fitted with a stirrer, dropping funnel, thermometer, and condenser with an attached nitrogen blanket.
  • the flask is charged with 192 grams (6.0 moles) of methanol and heated to 50C.
  • Freshly distilled p-dioxan-2-one (204 grams, 2.0 moles) is slowly added over a 30 minute period. After the addition is complete, the reaction mixture is stirred for 3 hours.
  • EXAMPLE 2 This example demonstrates the synthesis of an etherdiester by the catalyzed reaction of p-dioxan-Z-one with an aliphatic alcohol to yield the hydroxyetherester which is esterified to the desired etherdiester by an acid anhydride.
  • a l4flask is fitted with a stirrer, thermometer, dropping funnel, and condenser with an attached nitrogen blanket. The flask is charged with 192 grams (6.0 moles) of methanol and 1 gram of pyridine as catalyst. To this stirred mixture, heated at 50C., is added 204 grams (2.0 moles) of freshly distilled p-dioxan-2-one over a 30 minute period.
  • EXAMPLE 3 This example demonstrates the synthesis of an etherdiester by the reaction of p-dioxan-Z-one with isobutanol to yield the hydroxyetherester which is esterified with carboxylic acid.
  • the procedure in Example 1 is followed in this example by reaction of 192 grams (6.0 moles) of methanol with 204 grams (2.0 moles) of p-dioxan-2-one.
  • the product, methyl beta-hydroxyethoxyacetate is isolated in a 92 percent yield. Reaction of this product in 100 milliliters of benzene with 324 grams (2.0 moles) of 'n-butyric acid with 0.5 gram of para-toluenesulfonic acid catalyst is accomplished at reflux conditions.
  • EXAMPLE 6 This example further demonstrates the diversity in the synthesis of the ether-diesters by reactions of pdioxan-2-one with higher molecular weight alcohols and acids or acid anhydrides.
  • the procedure in Example 1 is followed in this reaction.
  • To 260 grams (2.0 moles) of 2-ethylhexanol at 100C. with one gram of tributylamine is slowly added 102 grams (1.0 mole) of p-dioxan-Z-one. After 8 hours the excess alcohol and catalyst are removed by distillation at reduced pressure.
  • To the residual product is added 297 grams (1.1 moles) of 2-ethylhexanoic anhydride. After this stirred mixture is heated at 100C.
  • EXAMPLE 7 This example demonstrates the use of an aliphatic alcohol, p-dioxan-Z-one and an aromatic acid to produce an ether-diester.
  • the procedure in Example 1 is followed.
  • Isobutanol 148 grams, 2.0 moles
  • 102 grams (1.0 mole) of p-dioxan-Z-one at 75C. to give a 92 percent yield to the isobutyl beta-hydroxyethoxyacetate.
  • This hydroxyetherester is reacted with 122 grams (1.0 mole) of benzoic acid in 50 milliliters of toluene and 0.3 gram of p-toluenesulfonic acid catalyst.
  • R is alkyl of from 1 to 8 carbon atoms and R is alkyl of from 1 to 7 carbon atoms.
  • a process for the production of ether-diesters having the formula wherein R is alkyl of from 1 to 8 carbon atoms and R is alkyl of from 1 to 7 carbon atoms or the phenyl moiety which comprises reacting p-dioxan-Z-one with an aliphatic alcohol having from 1 to 8 carbon atoms and subsequently esterifying the reaction product with an aliphatic carboxylic acid having from 2 to 8 carbon atoms or benzoic acid or an anhydride thereof.
  • the alcohol is selected from the group consisting of methanol, ethanol, propanol, n-butanol, isobutanol, 2-methylpentanol-l, n-hexanol, 2-ethylhexanol-l, n-octanol, allyl alcohol, and crotonyl alcohol.
  • a reaction according to claim 9 wherein the acid or base catalyst is selected from the group consisting of sulfuric acid, p-toluenesulfonic, organotin compounds, alkali metal hydroxides, pyridine, aliphatic tertiary amines, or N,N-dialkylanilines.
  • a process according to claim 7 wherein the mole ratio of alcohol to p-dioxanone is from about 1:1 to about 15:1, respectively.
  • a process according to claim 13 wherein the mole ratio of alcohol to p-dioxanone is from about 2:1 to about 7:1 respectively.
  • an acid anhydride selected from the group consisting of acetic, butyric, 2-methylpentanoic, hexanoic, 2-ethylhexanoic, octanoic and benzoic anhydride.
  • a process according to claim 7 wherein the mole ratio of intermediate hydroxylated ester to acid moiety is from about 1:1 to about 1:30, respectively.

Abstract

This invention relates to a new series of ether-diester derivatives of p-dioxanone having the formula

wherein R'' is alkyl of from 1 to 7 carbon atoms or the phenyl moiety and R is alkyl of from 1 to 8 carbon atoms. These novel compounds are produced by reacting p-dioxanone with an aliphatic alcohol having from 1 to 8 carbon atoms and esterifying the reaction product with an aliphatic carboxylic acid having from 2 to 8 carbon atoms or a corresponding acid anhydride. Benzoic acid or its anhydride yields the phenyl moiety in the ether-diester derivatives. The ether-diesters are particularly useful as plasticizers for polyvinyl chloride.

Description

[ 51 Dec. 30, 1975 ETHER DIESTER DERIVATIVES OF P-DIOXANONE Inventors: Thomas C. Snapp, Jr.; Alden E.
Blood, both of Longview, Tex.
[73] Assignee: Eastman Kodak Company,
Rochester, NY.
[22] Filed: Sept. 25, 1974 [2]] Appl. No.: 508,314
[52] US. Cl. 260/410.6; 260/476; 260/484 A [51] Int. Cl. C09F 5/08 [58] Field of Search 260/410.6, 484 A, 476
[56] References Cited UNITED STATES PATENTS 2,962,455 11/1960 Hostettler 260/484 A 3,086,044 4/1963 Kerschner.... 260/484 A 3,499,028 3/1970 McTeer 260/484 A 3,565,946 2/1971 Feng 260/484 A 3,689,531 9/1972 Critchfield... 260/484 A 3,767,627 10/1973 Schoen 260/484 A 3,776,766 12/1973 Smerz 260/410.6
Primary Examiner-Winston A. Douglas Assistant Examiner.lohn F. Neibling Attorney, Agent, or Firm-Edward R. Weber; Daniel B. Reece [ll [57] ABSTRACT This invention relates to a new series of ether-diester derivatives of p-dioxanone having the formula wherein R is alkyl of from 1 to 7 carbon atoms or the phenyl moiety and R is alkyl of from 1 to 8 carbon atoms. These novel compounds are produced by reacting p-dioxanone with an aliphatic alcohol having from 1 to 8 carbon atoms and esterifying the reaction product with an aliphatic carboxylic acid having from 2 to 8 carbon atoms or a corresponding acid anhydride. Benzoic acid or its anhydride yields the phenyl moiety in the ether-diester derivatives. The etherdiesters are particularly useful as plasticizers for polyvinyl chloride.
21 Claims, No Drawings ETHER DIESTER DERIVATIVES OF P-DIOXANONE This invention relates to a new family of chemical compounds, namely ether-diester derivatives of p-dioxanone. The new compounds have the following structural formula:
ll ll wherein R is alkyl of from 1 to 8 carbon atoms and R is alkyl of from 1 to 7 carbon atoms or the phenyl moiety.
The novel ether-diesters described herein result from the selective reaction of p-dioxan-2-one (p-dioxanone) with various aliphatic alcohols to yield an intermediate hydroxy ether-ester which can then be esterified. The highly selective reaction of p-dioxan-2-one with an alcohol is unexpected, since transesterification of the hydroxyetherester product with p-dioxanone could readily occur and p-dioxanone self-condensation would be a predicted side reaction. Neither the transesterification nor the self-condensation reaction is encountered in the synthesis of the ether-diesters.
The novel ether-diesters of this invention exhibit good utility in a broad range of applications. They have been found to be particularly effective plasticizers for polyvinyl chloride resin. The plasticizer properties of these compounds are characterized by good volatility and low temperature flexibility. Other application areas in which these compounds are useful include viscosity improvers for motor oil and brake fluid; and solvents in waxes, polishes and lubricants.
The novel ether-diesters are prepared by a two-step reaction sequence. It is believed that the reaction proceeds according to the following equations:
In the first step, an aliphatic alcohol is reacted with the p-dioxanone to afford nearly quantitative yields of alkyl beta-hydroxyethoxyacetate. This reaction is accomplished with an acid or basic catalyst to accelerate the reaction rate. Suitable catalysts for this reaction in clude sulfuric acid, organotin compounds (dibutyltin oxide, dibutyltin dilaurate, etc.), hydrochloric acid, zinc chloride, p-toluenesulfonic acid, pyridine, aliphatic tertiary amines, alkali metal hydroxides and N,N-dimethylaniline. However, the desired product can be produced in a noncatalyzed reaction between the two reactants. If catalysts are used, the catalyst concentration of from about 0.01 to about 2.0 weight percent, based on the total reactant weight, should be employed. A preferred catalyst concentration for this reaction is 0.1-1.0 weight percent of the total reactant weight. The reaction temperature at this stage should be from about 50C. to about 150C. The reaction can be conducted at a greater than atmospheric pressure without detrimental effects to the product. A mole ratio of alcohol to lactone can be from about 1:1 to about 15:1, respectively. A preferred ratio of reactants is from about 2:1 to about 7:1, respectively. The alcohol must be aliphatic and have a carbon skeleton of from 1 to 8 carbon atoms. Alcohols of particular importance are methanol, ethanol, propanol, n-butanol, isobutanol, 2-methylpentanol-l, 2-hexanol, 2-ethylhexanol-l, n-octanol, allyl alcohol and crotonyl alcohol.
The second step of the reaction sequence is the esterification of the intermediate alkyl beta-hydroxyethoxyacetate. Esteriflcation of the hydroxylated ether-ester can be accomplished by reaction with either a carboxylic acid or an acid anhydride. The carboxylic acid or anhydride is aliphatic in nature with a carbon chain of from 2 to 8 carbon atoms or aromatic with the phenyl moiety. The mole ratio of hydroxylated ester to acid moiety should be from about 10:10 to about 1.0230, respectively, to insure complete esterification of the p-dioxanone diester derivative.
Esteriflcation with an anhydride is achieved with or without catalysis at temperatures of from about 50C. to about 150C. However, esterification with the carboxylic acid requires a low concentration (from about 0.01 to about 1.0 weight percent based on total weight of the reactant) of acid catalyst to produce the desired diester product. Suitable acid catalysts are methanesulfonic acid, p-toluenesulfonic, phosphoric acid, sulfuric acid, hydrochloric acid, and zinc chloride. An azeotropic agent such as benzene, toluene, or hexane is useful to aid water removal during the reaction. Esterification temperatures with the acid should be from about 50C. to about 200C.
The novel ether-diesters are viscous, colorless liquids or low melting solids which can be distilled at reduced pressure without decomposition. Variation in physical properties (water and organic solubilities) can be readily obtained by modification of the carbon skeleton of the alcohol or acid utilized. This available range of properties renders these products particularly useful as coalescing agents and plasticizers in coating and resin applications.
The process of the invention is illustrated in greater detail by the following examples which are all conducted at atmospheric pressure, but it will be understood that these examples are not intended to limit the invention in any way and obvious modifications will occur to those skilled in the art.
EXAMPLE 1 This example demonstrates the synthesis of an etherdiester of p-dioxan-Z-one by the noncatalyzed reactions of an aliphatic alcohol, p-dioxan-2-one, and an acid anhydride. In this example a one-liter, four-neck flask is fitted with a stirrer, dropping funnel, thermometer, and condenser with an attached nitrogen blanket. The flask is charged with 192 grams (6.0 moles) of methanol and heated to 50C. Freshly distilled p-dioxan-2-one (204 grams, 2.0 moles) is slowly added over a 30 minute period. After the addition is complete, the reaction mixture is stirred for 3 hours. Excess methanol is removed by evaporation in vacuo to give a viscous, colorless liquid, methyl beta-hydroxyethoxyacetate, in a 95 percent yield. To this product, heated at 50C., is slowly added 214 grams (2.1 moles) of acetic anhydride. After stirring and heating at C. for 5 hours, the mixture is submitted to fractional distillation at 3 atmospheric pressure. The main fraction boils at l88l90C. and is identified as methyl beta-acetoxyethoxyacetate. Yield to this ether-diester is 93 percent. Structural determination is substantiated by infrared and NMR spectroscopy. Saponification equivalent of the product is 86 (theoretical is 88.1
EXAMPLE 2 This example demonstrates the synthesis of an etherdiester by the catalyzed reaction of p-dioxan-Z-one with an aliphatic alcohol to yield the hydroxyetherester which is esterified to the desired etherdiester by an acid anhydride. In this example a l4flask is fitted with a stirrer, thermometer, dropping funnel, and condenser with an attached nitrogen blanket. The flask is charged with 192 grams (6.0 moles) of methanol and 1 gram of pyridine as catalyst. To this stirred mixture, heated at 50C., is added 204 grams (2.0 moles) of freshly distilled p-dioxan-2-one over a 30 minute period. The resulting reaction mixture is stirred for 30 hours at 50C. after which excess methanol and pyridine are removed by evaporation in vacuo to give methyl betahydroxyethoxyacetate in a 93 percent yield. To this stirred product mixed with 1 gram of pyridine at 50C. is slowly added 214 grams (2.1 moles) of acetic anhydride. After five hours the reaction mixture is submitted to fractional distillation at atmospheric pressure. The main fraction is methyl beta-acetoxyethoxyacetate which distills at 188190C. Yield to this ether-diester from the hydroxyetherester is 90 percent. Saponification equivalent of product is analyzed to be 86.5 (theoretical is 88.1
EXAMPLE 3 This example demonstrates the synthesis of an etherdiester by the reaction of p-dioxan-Z-one with isobutanol to yield the hydroxyetherester which is esterified with carboxylic acid. The procedure in Example 1 is followed in this example by reaction of 192 grams (6.0 moles) of methanol with 204 grams (2.0 moles) of p-dioxan-2-one. The product, methyl beta-hydroxyethoxyacetate, is isolated in a 92 percent yield. Reaction of this product in 100 milliliters of benzene with 324 grams (2.0 moles) of 'n-butyric acid with 0.5 gram of para-toluenesulfonic acid catalyst is accomplished at reflux conditions. After collection of 18 milliliters of water, the reaction mixture is cooled and treated with 15 grams of sodium carbonate. After filtration and fractional distillation at reduced pressure the methyl 2-n-butyryloxyethoxyacetate is distilled at 105l 18C. at 1 mm. mercury pressure in an 89 percent yield. Saponification equivalent of this product analyzes to be 100 (theoretical is 102).
cn cmciijocu cu oci-i ljocH EXAMPLE 4 CH CH CH COCH C H OCH COCH CHCH EXAMPLE 5 This example demonstrates the diversity in the synthesis of ether-diesters by reactions of p-dioxan2-one, butanol, and 2-ethylhexanoic anhydride. The procedure in Example 1 is followed in this preparation. To 370 grams (5.0 moles) of n-butanol at C. is slowly added 102 grams 1.0 mole) of p-dioxan2-one. After 5 hours the excess butanol is removed by evaporation at reduced pressure. To the residual product is added 297 grams 1.1 moles) of 2-ethylhexanoic anhydride. After this stirred mixture is heated at C. for 6 hours, the mixture is distilled at reduced pressure to give an 87 percent yield of n-butyl 2-(2-ethylhexyryloxy)ethoxyacetate, boiling point is 153154C. at 1 mm. mercury pressure. Saponification equivalent analysis is 148.6 (theoretical is 150.5). Infrared spectroscopy verifies the ether-diester synthesis.
EXAMPLE 6 This example further demonstrates the diversity in the synthesis of the ether-diesters by reactions of pdioxan-2-one with higher molecular weight alcohols and acids or acid anhydrides. The procedure in Example 1 is followed in this reaction. To 260 grams (2.0 moles) of 2-ethylhexanol at 100C. with one gram of tributylamine is slowly added 102 grams (1.0 mole) of p-dioxan-Z-one. After 8 hours the excess alcohol and catalyst are removed by distillation at reduced pressure. To the residual product is added 297 grams (1.1 moles) of 2-ethylhexanoic anhydride. After this stirred mixture is heated at 100C. for 6 hours, the mixture is distilled to give an 84 percent yield of Z-ethylhexyl 2-(2-ethy1hexyryloxy)ethoxyacetate with a boiling point of l67169C. at 1 mm mercury pressure. Saponification equivalent analysis is 177.2 (theoretical is 179). Infrared and nuclear magnetic resonance spectroscopy verifies the ether-diester synthesis.
EXAMPLE 7 This example demonstrates the use of an aliphatic alcohol, p-dioxan-Z-one and an aromatic acid to produce an ether-diester. The procedure in Example 1 is followed. Isobutanol (148 grams, 2.0 moles) is reacted with 102 grams (1.0 mole) of p-dioxan-Z-one at 75C. to give a 92 percent yield to the isobutyl beta-hydroxyethoxyacetate. This hydroxyetherester is reacted with 122 grams (1.0 mole) of benzoic acid in 50 milliliters of toluene and 0.3 gram of p-toluenesulfonic acid catalyst. After removal of 18 milliliters of water, the reaction mixture is cooled and treated with 10 grams of calcium carbonate to neutralize acidic residues. After filtration and fractional distillation at reduced pressure the isobutyl benzoyloxyethoxyacetate product is isolated in an 86 percent yield. Saponification equivalent analysis of the viscous, semisolid colorless product is 138.5 (theoretical is 140). Infrared and nuclear magnetic reso nance spectroscopy verifies the ether-diester synthesis.
The invention has been described in detail with particular reference to preferred embodiments thereof, but it will be understood that variations and modifications can be effected within the spirit and scope of the invention as described hereinabove.
We claim:
1. A compound having the formula wherein R is alkyl of from 1 to 8 carbon atoms and R is alkyl of from 1 to 7 carbon atoms.
2. The ether-diester in claim 1 wherein R is CH and R is C l-l 3. The ether-diester in claim 1 wherein both R and R are C H 4. The ether-diester in claim 1 wherein R is C H and R is C H 5. The ether-diester in claim 1 wherein R is C l-l and R is C l-l 6. The ether-diester in claim 1 wherein R is C H and R is phenyl.
7. A process for the production of ether-diesters having the formula wherein R is alkyl of from 1 to 8 carbon atoms and R is alkyl of from 1 to 7 carbon atoms or the phenyl moiety, which comprises reacting p-dioxan-Z-one with an aliphatic alcohol having from 1 to 8 carbon atoms and subsequently esterifying the reaction product with an aliphatic carboxylic acid having from 2 to 8 carbon atoms or benzoic acid or an anhydride thereof.
8. A process according to claim 7 wherein the alcohol is selected from the group consisting of methanol, ethanol, propanol, n-butanol, isobutanol, 2-methylpentanol-l, n-hexanol, 2-ethylhexanol-l, n-octanol, allyl alcohol, and crotonyl alcohol.
9. A process according to claim 7 wherein the reaction of the p-dioxanone and alcohol is conducted in the presence of a catalyst.
10. A reaction according to claim 9 wherein the acid or base catalyst is selected from the group consisting of sulfuric acid, p-toluenesulfonic, organotin compounds, alkali metal hydroxides, pyridine, aliphatic tertiary amines, or N,N-dialkylanilines.
11. A reaction according to claim 9 wherein the catalyst is present in a concentration of from about 0.01 percent to about 2.0 percent based upon the total weight of the reactant.
12. A process according to claim 7 wherein the reaction of p-dioxanone and alcohol is conducted at a temperature from about 50C. to 150C.
13. A process according to claim 7 wherein the mole ratio of alcohol to p-dioxanone is from about 1:1 to about 15:1, respectively.
14. A process according to claim 13 wherein the mole ratio of alcohol to p-dioxanone is from about 2:1 to about 7:1 respectively. A
15. A process according to claim 7 wherein the esterification reaction is conducted with a carboxylic acid selected from the group consisting of acetic, butyric, Z-methylpentanoic, hexanoic, 2-ethylhexanoic, octanoic, and benzoic acid.
16. A process according to claim 15 wherein the esterification is conducted in the presence of a catalyst selected from the group consisting of methanesulfonic, toluenesulfonic, sulfuric, phosphoric, or hydrochloric acid.
17. A process according to claim 16 wherein an esterification catalyst is present in an amount of from about 0.01 weight percent to about 1.0 weight percent based upon the total weight of the reactants.
18. A process according to claim 7 wherein the esterification reaction is conducted with an acid anhydride selected from the group consisting of acetic, butyric, 2-methylpentanoic, hexanoic, 2-ethylhexanoic, octanoic and benzoic anhydride.
19. A process according to claim 18 wherein the esterification is conducted at a temperature of from about 50C. to about 150C.
20. A process according to claim 15 wherein the esterification reaction is conducted at a temperature of from about C. to about 200C.
21. A process according to claim 7 wherein the mole ratio of intermediate hydroxylated ester to acid moiety is from about 1:1 to about 1:30, respectively.

Claims (21)

1. A COMPOUND HAVING THE FORMULA
2. The ether-diester in claim 1 wherein R is CH3 and R'' is -C4H9.
3. The ether-diester in claim 1 wherein both R and R'' are -C4H9.
4. The ether-diester in claim 1 wherein R is -C4H9 and R'' is -C7H15.
5. The ether-diester in claim 1 wherein R is C8H17 and R'' is C7H15.
6. The ether-diester in claim 1 wherein R is -C4H9 and R'' is phenyl.
7. A process for the production of ether-diesters having the formula
8. A process according to claim 7 wherein the alcohol is selected from the group consisting of methanol, ethanol, propanol, n-butanol, isobutanol, 2-methylpentanol-1, n-hexanol, 2-ethylhexanol-1, n-octanol, allyl alcohol, and crotonyl alcohol.
9. A process according to claim 7 wherein the reaction of the p-dioxanone and alcohol is conducted in the presence of a catalyst.
10. A reaction according to claim 9 wherein the acid or base catalyst is selected from the group consisting of sulfuric acid, p-toluenesulfonic, organotin compounds, alkali metal hydroxides, pyridine, aliphatic tertiary amines, or N,N-dialkylanilines.
11. A reaction according to claim 9 wherein the catalyst is present in a concentration of from about 0.01 percent to about 2.0 percent based upon the total weight of the reactant.
12. A process according to claim 7 wherein the reaction of p-dioxanone and alcohol is conducted at a temperature from about 50*C. to 150*C.
13. A process according to claim 7 wherein the mole ratio of alcohol to p-dioxanone is from about 1:1 to about 15:1, respectively.
14. A process according to claim 13 wherein the mole ratio of alcohol to p-dioxanone is from about 2:1 to about 7:1, respectively.
15. A process according to claim 7 wherein the esterification reaction is conducted with a carboxylic acid selected from the group consisting of acetic, butyric, 2-methylpentanoic, hexanoic, 2-ethylhexanoic, octanoic, and benzoic acid.
16. A process according to claim 15 wherein the esterification is conducted in the presence of a catalyst selected from the group consisting of methanesulfonic, toluenesulfonic, sulfuric, phosphoric, or hydrochloric acid.
17. A process according to claim 16 wherein an esterification catalyst is present in an amount of from about 0.01 weight percent to about 1.0 weight percent based upon the total weight of the reactants.
18. A process according to claim 7 wherein the esterification reaction is conducted with an acid anhydride selected from the group consisting of acetic, butyric, 2-methylpentanoic, hexanoic, 2-ethylhexanoic, octanoic and benzoic anhydride.
19. A process according to claim 18 wherein the esterification is conducted at a temperature of from about 50*C. to about 150*C.
20. A process according to claim 15 wherein the esterification reaction is conducted at a temperature of from about 75*C. to about 200*C.
21. A process according to claim 7 wherein the mole ratio of intermediate hydroxylated ester to acid moiety is from about 1:1 to about 1:3.0, respectively.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4668433A (en) * 1984-08-06 1987-05-26 Givaudan Corporation Novel derivatives of 6-hydroxyhexanoates as fragrance ingredients
US20050234121A1 (en) * 2004-03-24 2005-10-20 Binder Thomas P Vegetable based dioxanone derivatives, synthesis and uses thereof
KR100948498B1 (en) 2008-04-10 2010-03-23 한국화학연구원 An alkyl 2-t-butoxyethoxy-acetate compound and a method for preparing the same

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2962455A (en) * 1957-04-18 1960-11-29 Union Carbide Corp Cellular polyurethane resins and preparation of same
US3086044A (en) * 1960-05-27 1963-04-16 Cities Service Res & Dev Co Method of preparing complex diesters of a dibasic acid with a diol and an excess of a monohydric alcohol
US3499028A (en) * 1965-05-25 1970-03-03 Union Carbide Corp Di(1-acyloxyaliphatic) ethers and derivatives thereof
US3565946A (en) * 1963-02-21 1971-02-23 Exxon Research Engineering Co Polymeric materials and the preparation thereof
US3689531A (en) * 1969-04-01 1972-09-05 Union Carbide Corp Copolymers of lactones and alkylene oxides
US3767627A (en) * 1970-12-10 1973-10-23 Stamicarbon Preparation of polylactones having ester end groups
US3776766A (en) * 1970-11-18 1973-12-04 Hoechst Ag Process for improving the processing properties of polyester filaments and fibres

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2962455A (en) * 1957-04-18 1960-11-29 Union Carbide Corp Cellular polyurethane resins and preparation of same
US3086044A (en) * 1960-05-27 1963-04-16 Cities Service Res & Dev Co Method of preparing complex diesters of a dibasic acid with a diol and an excess of a monohydric alcohol
US3565946A (en) * 1963-02-21 1971-02-23 Exxon Research Engineering Co Polymeric materials and the preparation thereof
US3499028A (en) * 1965-05-25 1970-03-03 Union Carbide Corp Di(1-acyloxyaliphatic) ethers and derivatives thereof
US3689531A (en) * 1969-04-01 1972-09-05 Union Carbide Corp Copolymers of lactones and alkylene oxides
US3776766A (en) * 1970-11-18 1973-12-04 Hoechst Ag Process for improving the processing properties of polyester filaments and fibres
US3767627A (en) * 1970-12-10 1973-10-23 Stamicarbon Preparation of polylactones having ester end groups

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4668433A (en) * 1984-08-06 1987-05-26 Givaudan Corporation Novel derivatives of 6-hydroxyhexanoates as fragrance ingredients
US20050234121A1 (en) * 2004-03-24 2005-10-20 Binder Thomas P Vegetable based dioxanone derivatives, synthesis and uses thereof
US7754823B2 (en) 2004-03-24 2010-07-13 Archer-Daniels-Midland Company Vegetable based dioxanone derivatives, synthesis and uses thereof
KR100948498B1 (en) 2008-04-10 2010-03-23 한국화학연구원 An alkyl 2-t-butoxyethoxy-acetate compound and a method for preparing the same

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